美国药品NDC（国家药品编码）与药品说明书数据库（U.S. FDA National Drug Code DataBase）

NDC包装代码	产品NDC	产品类型	商品名	通用名	剂型	给药途径	上市日期	结束日期	市场类别	申请号	标签持有者	活性成分	规格	包装描述
71205-368-60	71205-368	HUMAN PRESCRIPTION DRUG	metoprolol succinate	metoprolol succinate	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20191203	N/A	ANDA	ANDA204161	Proficient Rx LP	METOPROLOL SUCCINATE	25 mg/1	60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71205-368-60)
71205-368-90	71205-368	HUMAN PRESCRIPTION DRUG	metoprolol succinate	metoprolol succinate	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20191203	N/A	ANDA	ANDA204161	Proficient Rx LP	METOPROLOL SUCCINATE	25 mg/1	90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71205-368-90)
53002-2612-0	53002-2612	HUMAN PRESCRIPTION DRUG	metoprolol succinate	metoprolol succinate	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20211231	N/A	ANDA	ANDA204161	RPK Pharmaceuticals, Inc.	METOPROLOL SUCCINATE	50 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (53002-2612-0)
53002-2612-3	53002-2612	HUMAN PRESCRIPTION DRUG	metoprolol succinate	metoprolol succinate	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20211231	N/A	ANDA	ANDA204161	RPK Pharmaceuticals, Inc.	METOPROLOL SUCCINATE	50 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (53002-2612-3)
53002-2781-0	53002-2781	HUMAN PRESCRIPTION DRUG	metoprolol succinate	metoprolol succinate	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20211231	N/A	ANDA	ANDA204161	RPK Pharmaceuticals, Inc.	METOPROLOL SUCCINATE	25 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (53002-2781-0)
53002-2781-3	53002-2781	HUMAN PRESCRIPTION DRUG	metoprolol succinate	metoprolol succinate	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20211231	N/A	ANDA	ANDA204161	RPK Pharmaceuticals, Inc.	METOPROLOL SUCCINATE	25 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (53002-2781-3)